MELAS Missed for Years: Stroke-Like Lesions Are No Indication for Brain Biopsy.

IF 0.9 Q4 CLINICAL NEUROLOGY
Case Reports in Neurological Medicine Pub Date : 2019-12-27 eCollection Date: 2019-01-01 DOI:10.1155/2019/9312451
J Finsterer
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引用次数: 1

Abstract

A 56-year-old female with a history of chronic alcoholism until age 38 y with a relapse between ages 45 and 46 y developed seizures, psychosis, and hemianopia to the left at age 46 y. Imaging revealed a right parieto-occipital lesion with intralesional bleeding. Five months after the first lesion she developed a second left parieto-occipital lesion, resulting in cortical blindness. Extensive workup, including brain biopsy, was noninformative. Retrospectively, the occipital abnormalities were identified as stroke-like lesions (SLLs). Further manifestations of the mitochondrial disorder (MID) were tremor, cerebral atrophy, bilateral basal ganglia, calcification, glaucoma, hypoacusis, short stature, hyperostosis frontalis, hyperthyroidism, sick-sinus syndrome and AV-block-1, and myopathy. According to the Walker criteria, a possible MID was diagnosed. In conclusion, adult-onset MID may be missed for years, SLLs may be easily misinterpreted entailing brain biopsy, and psychosis may contribute to a reduced impact for proper workup of a MID.

Abstract Image

MELAS被遗漏多年:脑卒中样病变没有脑活检的迹象。
56岁女性,38岁前有慢性酒精中毒史,45岁至46岁复发,46岁时出现癫痫发作、精神错乱和偏左偏盲。影像显示右侧顶骨至枕部病变伴病灶内出血。第一次病变发生5个月后,她出现了第二次左顶骨-枕部病变,导致皮质性失明。广泛的检查,包括脑活检,没有提供任何信息。回顾性分析,枕部异常被确定为卒中样病变(SLLs)。线粒体疾病(MID)的进一步表现为震颤、脑萎缩、双侧基底神经节、钙化、青光眼、听觉减退、身材矮小、额部肥厚、甲状腺功能亢进、病窦综合征和AV-block-1以及肌病。根据沃克标准,诊断为可能的MID。总之,成人发病的MID可能会被遗漏多年,sll可能很容易被误解,需要进行脑活检,精神病可能会降低对MID适当检查的影响。
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